The following data is part of a premarket notification filed by Steris Corporation with the FDA for Amsco Surgical Table.
| Device ID | K971307 |
| 510k Number | K971307 |
| Device Name: | AMSCO SURGICAL TABLE |
| Classification | Table, Operating-room, Ac-powered |
| Applicant | STERIS Corporation 5960 HEISLEY RD. Mentor, OH 44060 |
| Contact | Matthew M Hull |
| Correspondent | Matthew M Hull STERIS Corporation 5960 HEISLEY RD. Mentor, OH 44060 |
| Product Code | FQO |
| CFR Regulation Number | 878.4960 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1997-04-08 |
| Decision Date | 1997-06-27 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00724995155346 | K971307 | 000 |
| 00724995155025 | K971307 | 000 |
| 00724995155032 | K971307 | 000 |
| 00724995155049 | K971307 | 000 |
| 00724995155056 | K971307 | 000 |
| 00724995155063 | K971307 | 000 |
| 00724995155070 | K971307 | 000 |
| 00724995155087 | K971307 | 000 |
| 00724995155094 | K971307 | 000 |
| 00724995155117 | K971307 | 000 |
| 00724995155131 | K971307 | 000 |
| 00724995155315 | K971307 | 000 |
| 00724995155322 | K971307 | 000 |
| 00724995155339 | K971307 | 000 |
| 00724995164508 | K971307 | 000 |